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                                       Details for article 16 of 16 found articles
 
 
  Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia
 
 
Title: Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia
Author: Zhang, Tingting
Wu, Jing
Zhao, Xiaoxue
Hou, Feifei
Ma, Tengfei
Wang, Huijuan
Zhang, Xu
Zhang, Xiangyu
Appeared in: Archives of oral biology
Paging: Volume 100 (2019) nr. C pages 49-56
Year: 2019
Contents:
Publisher: Elsevier Ltd
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 16 of 16 found articles
 
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